Methionine restriction decreases visceral fat mass and preserves insulin action in aging male Fischer 344 rats independent of energy restriction
Summary Reduced dietary methionine intake (0.17% methionine, MR) and calorie restriction (CR) prolong lifespan in male Fischer 344 rats. Although the mechanisms are unclear, both regimens feature lower body weight and reductions in adiposity. Reduced fat deposition in CR is linked to preservation of...
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description | Summary
Reduced dietary methionine intake (0.17% methionine, MR) and calorie restriction (CR) prolong lifespan in male Fischer 344 rats. Although the mechanisms are unclear, both regimens feature lower body weight and reductions in adiposity. Reduced fat deposition in CR is linked to preservation of insulin responsiveness in older animals. These studies examine the relationship between insulin responsiveness and visceral fat in MR and test whether, despite lower food intake observed in MR animals, decreased visceral fat accretion and preservation of insulin sensitivity is not secondary to CR. Accordingly, rats pair fed (pf) control diet (0.86% methinone, CF) to match the food intake of MR for 80 weeks exhibit insulin, glucose, and leptin levels similar to control‐fed animals and comparable amounts of visceral fat. Conversely, MR rats show significantly reduced visceral fat compared to CF and PF with concomitant decreases in basal insulin, glucose, and leptin, and increased adiponectin and triiodothyronine. Daily energy expenditure in MR animals significantly exceeds that of both PF and CF. In a separate cohort, insulin responses of older MR animals as measured by oral glucose challenge are similar to young animals. Longitudinal assessments of MR and CF through 112 weeks of age reveal that MR prevents age‐associated increases in serum lipids. By 16 weeks, MR animals show a 40% reduction in insulin‐like growth factor‐1 (IGF‐1) that is sustained throughout life; CF IGF‐1 levels decline much later, beginning at 112 weeks. Collectively, the results indicate that MR reduces visceral fat and preserves insulin activity in aging rats independent of energy restriction. |
doi_str_mv | 10.1111/j.1474-9726.2006.00220.x |
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Reduced dietary methionine intake (0.17% methionine, MR) and calorie restriction (CR) prolong lifespan in male Fischer 344 rats. Although the mechanisms are unclear, both regimens feature lower body weight and reductions in adiposity. Reduced fat deposition in CR is linked to preservation of insulin responsiveness in older animals. These studies examine the relationship between insulin responsiveness and visceral fat in MR and test whether, despite lower food intake observed in MR animals, decreased visceral fat accretion and preservation of insulin sensitivity is not secondary to CR. Accordingly, rats pair fed (pf) control diet (0.86% methinone, CF) to match the food intake of MR for 80 weeks exhibit insulin, glucose, and leptin levels similar to control‐fed animals and comparable amounts of visceral fat. Conversely, MR rats show significantly reduced visceral fat compared to CF and PF with concomitant decreases in basal insulin, glucose, and leptin, and increased adiponectin and triiodothyronine. Daily energy expenditure in MR animals significantly exceeds that of both PF and CF. In a separate cohort, insulin responses of older MR animals as measured by oral glucose challenge are similar to young animals. Longitudinal assessments of MR and CF through 112 weeks of age reveal that MR prevents age‐associated increases in serum lipids. By 16 weeks, MR animals show a 40% reduction in insulin‐like growth factor‐1 (IGF‐1) that is sustained throughout life; CF IGF‐1 levels decline much later, beginning at 112 weeks. Collectively, the results indicate that MR reduces visceral fat and preserves insulin activity in aging rats independent of energy restriction.</description><identifier>ISSN: 1474-9718</identifier><identifier>EISSN: 1474-9726</identifier><identifier>DOI: 10.1111/j.1474-9726.2006.00220.x</identifier><identifier>PMID: 16800846</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>adipose ; Adipose Tissue - drug effects ; Adiposity ; Aging ; Animals ; Body Composition - drug effects ; Body Weight - drug effects ; Cholesterol - metabolism ; energy expenditure ; Energy Intake ; Energy Metabolism - drug effects ; Glucose Tolerance Test ; insulin ; Insulin - blood ; Insulin-Like Growth Factor I - metabolism ; Male ; Methionine - deficiency ; methionine restriction ; Rats ; Rats, Inbred F344 ; Time Factors ; Triglycerides - metabolism</subject><ispartof>Aging cell, 2006-08, Vol.5 (4), p.305-314</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4830-4eff25ab2f52648cc52e1363ba5919d3189bd038662cc4ebba2585945835ab4c3</citedby><cites>FETCH-LOGICAL-c4830-4eff25ab2f52648cc52e1363ba5919d3189bd038662cc4ebba2585945835ab4c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1474-9726.2006.00220.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1474-9726.2006.00220.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,11571,27933,27934,45583,45584,46061,46485</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1474-9726.2006.00220.x$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16800846$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Malloy, Virginia L.</creatorcontrib><creatorcontrib>Krajcik, Rozlyn A.</creatorcontrib><creatorcontrib>Bailey, Steven J.</creatorcontrib><creatorcontrib>Hristopoulos, George</creatorcontrib><creatorcontrib>Plummer, Jason D.</creatorcontrib><creatorcontrib>Orentreich, Norman</creatorcontrib><title>Methionine restriction decreases visceral fat mass and preserves insulin action in aging male Fischer 344 rats independent of energy restriction</title><title>Aging cell</title><addtitle>Aging Cell</addtitle><description>Summary
Reduced dietary methionine intake (0.17% methionine, MR) and calorie restriction (CR) prolong lifespan in male Fischer 344 rats. Although the mechanisms are unclear, both regimens feature lower body weight and reductions in adiposity. Reduced fat deposition in CR is linked to preservation of insulin responsiveness in older animals. These studies examine the relationship between insulin responsiveness and visceral fat in MR and test whether, despite lower food intake observed in MR animals, decreased visceral fat accretion and preservation of insulin sensitivity is not secondary to CR. Accordingly, rats pair fed (pf) control diet (0.86% methinone, CF) to match the food intake of MR for 80 weeks exhibit insulin, glucose, and leptin levels similar to control‐fed animals and comparable amounts of visceral fat. Conversely, MR rats show significantly reduced visceral fat compared to CF and PF with concomitant decreases in basal insulin, glucose, and leptin, and increased adiponectin and triiodothyronine. Daily energy expenditure in MR animals significantly exceeds that of both PF and CF. In a separate cohort, insulin responses of older MR animals as measured by oral glucose challenge are similar to young animals. Longitudinal assessments of MR and CF through 112 weeks of age reveal that MR prevents age‐associated increases in serum lipids. By 16 weeks, MR animals show a 40% reduction in insulin‐like growth factor‐1 (IGF‐1) that is sustained throughout life; CF IGF‐1 levels decline much later, beginning at 112 weeks. Collectively, the results indicate that MR reduces visceral fat and preserves insulin activity in aging rats independent of energy restriction.</description><subject>adipose</subject><subject>Adipose Tissue - drug effects</subject><subject>Adiposity</subject><subject>Aging</subject><subject>Animals</subject><subject>Body Composition - drug effects</subject><subject>Body Weight - drug effects</subject><subject>Cholesterol - metabolism</subject><subject>energy expenditure</subject><subject>Energy Intake</subject><subject>Energy Metabolism - drug effects</subject><subject>Glucose Tolerance Test</subject><subject>insulin</subject><subject>Insulin - blood</subject><subject>Insulin-Like Growth Factor I - metabolism</subject><subject>Male</subject><subject>Methionine - deficiency</subject><subject>methionine restriction</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><subject>Time Factors</subject><subject>Triglycerides - metabolism</subject><issn>1474-9718</issn><issn>1474-9726</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctOwzAQRS0E4v0LyCt2DX7FdRYsqoqXVMQG1pbjTFpXqVPstNC_4JNxaFVY4oV9rTl3RjODEKYko-nczDMqhmJQDJnMGCEyI4Qxkn0eoNN94HCvqTpBZzHOCaHDgvBjdEKlIkQJeYq-nqGbudY7DzhA7IKzXfriCmwAEyHitYsWgmlwbTq8MDFi4yu8TDCEdYo7H1eN89hsjb2aOj9NaAP4PplnEDAXAgfT9XQFS0iX73BbY_AQppu_lS_QUW2aCJe79xy93d-9jh8Hk5eHp_FoMrBCcTIQUNcsNyWrcyaFsjZnQLnkpckLWlScqqKsCFdSMmsFlKVhucoLkSueXMLyc3S9zbsM7fsq1deLvtGmMR7aVdRSDSWhRCZQbUEb2hgD1HoZ3MKEjaZE99vQc90PWvdD1_029M829GeyXu1qrMoFVL_G3fgTcLsFPlwDm38n1qPx3SQp_g1nHpsw</recordid><startdate>200608</startdate><enddate>200608</enddate><creator>Malloy, Virginia L.</creator><creator>Krajcik, Rozlyn A.</creator><creator>Bailey, Steven J.</creator><creator>Hristopoulos, George</creator><creator>Plummer, Jason D.</creator><creator>Orentreich, Norman</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200608</creationdate><title>Methionine restriction decreases visceral fat mass and preserves insulin action in aging male Fischer 344 rats independent of energy restriction</title><author>Malloy, Virginia L. ; Krajcik, Rozlyn A. ; Bailey, Steven J. ; Hristopoulos, George ; Plummer, Jason D. ; Orentreich, Norman</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4830-4eff25ab2f52648cc52e1363ba5919d3189bd038662cc4ebba2585945835ab4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>adipose</topic><topic>Adipose Tissue - drug effects</topic><topic>Adiposity</topic><topic>Aging</topic><topic>Animals</topic><topic>Body Composition - drug effects</topic><topic>Body Weight - drug effects</topic><topic>Cholesterol - metabolism</topic><topic>energy expenditure</topic><topic>Energy Intake</topic><topic>Energy Metabolism - drug effects</topic><topic>Glucose Tolerance Test</topic><topic>insulin</topic><topic>Insulin - blood</topic><topic>Insulin-Like Growth Factor I - metabolism</topic><topic>Male</topic><topic>Methionine - deficiency</topic><topic>methionine restriction</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Time Factors</topic><topic>Triglycerides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Malloy, Virginia L.</creatorcontrib><creatorcontrib>Krajcik, Rozlyn A.</creatorcontrib><creatorcontrib>Bailey, Steven J.</creatorcontrib><creatorcontrib>Hristopoulos, George</creatorcontrib><creatorcontrib>Plummer, Jason D.</creatorcontrib><creatorcontrib>Orentreich, Norman</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Aging cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Malloy, Virginia L.</au><au>Krajcik, Rozlyn A.</au><au>Bailey, Steven J.</au><au>Hristopoulos, George</au><au>Plummer, Jason D.</au><au>Orentreich, Norman</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methionine restriction decreases visceral fat mass and preserves insulin action in aging male Fischer 344 rats independent of energy restriction</atitle><jtitle>Aging cell</jtitle><addtitle>Aging Cell</addtitle><date>2006-08</date><risdate>2006</risdate><volume>5</volume><issue>4</issue><spage>305</spage><epage>314</epage><pages>305-314</pages><issn>1474-9718</issn><eissn>1474-9726</eissn><abstract>Summary
Reduced dietary methionine intake (0.17% methionine, MR) and calorie restriction (CR) prolong lifespan in male Fischer 344 rats. Although the mechanisms are unclear, both regimens feature lower body weight and reductions in adiposity. Reduced fat deposition in CR is linked to preservation of insulin responsiveness in older animals. These studies examine the relationship between insulin responsiveness and visceral fat in MR and test whether, despite lower food intake observed in MR animals, decreased visceral fat accretion and preservation of insulin sensitivity is not secondary to CR. Accordingly, rats pair fed (pf) control diet (0.86% methinone, CF) to match the food intake of MR for 80 weeks exhibit insulin, glucose, and leptin levels similar to control‐fed animals and comparable amounts of visceral fat. Conversely, MR rats show significantly reduced visceral fat compared to CF and PF with concomitant decreases in basal insulin, glucose, and leptin, and increased adiponectin and triiodothyronine. Daily energy expenditure in MR animals significantly exceeds that of both PF and CF. In a separate cohort, insulin responses of older MR animals as measured by oral glucose challenge are similar to young animals. Longitudinal assessments of MR and CF through 112 weeks of age reveal that MR prevents age‐associated increases in serum lipids. By 16 weeks, MR animals show a 40% reduction in insulin‐like growth factor‐1 (IGF‐1) that is sustained throughout life; CF IGF‐1 levels decline much later, beginning at 112 weeks. Collectively, the results indicate that MR reduces visceral fat and preserves insulin activity in aging rats independent of energy restriction.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>16800846</pmid><doi>10.1111/j.1474-9726.2006.00220.x</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | adipose Adipose Tissue - drug effects Adiposity Aging Animals Body Composition - drug effects Body Weight - drug effects Cholesterol - metabolism energy expenditure Energy Intake Energy Metabolism - drug effects Glucose Tolerance Test insulin Insulin - blood Insulin-Like Growth Factor I - metabolism Male Methionine - deficiency methionine restriction Rats Rats, Inbred F344 Time Factors Triglycerides - metabolism |
title | Methionine restriction decreases visceral fat mass and preserves insulin action in aging male Fischer 344 rats independent of energy restriction |
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